MeSH Browser

MeSH Supplementary: Glutathione synthetase deficiency
Unique ID: C536835
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536835
Entry Term(s): 5-oxoprolinemia; 5-oxoprolinuria; Deficiency of Glutathione Synthase; Deficiency of Glutathione Synthetase; Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to; Pyroglutamic Acidemia; Pyroglutamic aciduria
Registry Number: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; Glutathione Synthase / *deficiency
Frequency: 28
Date of Entry: 2010/08/25
Revision Date: 2019/07/01

Concept UI: M0531296
Registry Number: 0
Terms: Glutathione synthetase deficiency Preferred Term
Term UI T740593
Date02/24/2009
LexicalTag NON
ThesaurusID; 5-oxoprolinuria
Term UI T740595
Date02/24/2009
LexicalTag NON
ThesaurusID; Pyroglutamic Acidemia
Term UI T841515
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Deficiency of Glutathione Synthase
Term UI T841513
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Deficiency of Glutathione Synthetase
Term UI T841514
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); 5-oxoprolinemia
Term UI T740597
Date02/24/2009
LexicalTag NON
ThesaurusID; Pyroglutamic aciduria
Term UI T740594
Date02/24/2009
LexicalTag NON
ThesaurusID

Glutathione synthetase deficiency MeSH Supplementary Concept Data 2024